Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresis. [electronic resource]
Producer: 19971208Description: 2121-7 p. digitalISSN:- 0009-9147
- Adrenal Hyperplasia, Congenital
- Alleles
- Benzothiazoles
- Diamines
- Electrophoresis, Capillary
- Female
- Fluorescent Dyes
- Gene Amplification
- Humans
- Lasers
- Male
- Organic Chemicals
- Point Mutation
- Polymerase Chain Reaction
- Quinolines
- Reproducibility of Results
- Sensitivity and Specificity
- Spectrometry, Fluorescence
- Steroid 21-Hydroxylase -- genetics
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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